نتایج جستجو برای: idiopathic osteosclerosis

تعداد نتایج: 63468  

2013
M Moeini M Moeini N Lotfizadeh M Alavi

BACKGROUND Bisphosphonates‎ inhibit osteoclasts, prevent bone resorption and decrease bone turnover. This study examined radiography finding in bisphosphonate-associated osteonecrosis of jaws. MATERIALS AND METHODS This is a retrospective series of 12 clinically diagnosed patients between 7 to 21 year old (average 13 years). They required emergency dental conditions requiring management by de...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه گیلان - دانشکده علوم پایه 1390

ناباروری به عدم توفیق زوجین در بارداری پس از گذشت یکسال از مقاربت های متوالی بدون استفاده از وسایل پیشگیری از بارداری گفته می شود. ناباروری در مردان یک سندرم چند عاملی به شمار می آید که دلایل ژنتیکی و غیر ژنتیکی متعددی می تواند داشته باشد. ناباروری idiopathic به نوعی از ناباروری اطلاق می شود که دلایل آن نامشخص است. وقوع جهش در یک g_protein coupled receptor به نام gpr54 منجر به بروز ihh می شود. ...

Journal: :The Journal of the Japanese Association for Chest Surgery 2007

Journal: :Haematologica 2007
Ayalew Tefferi

recommended the use of the name primary myelofibrosis (PMF) for the clinicopathologic entity otherwise known as chronic idiopathic myelofibrosis, agnogenic myeloid metaplasia, or myelofibrosis with myeloid metaplasia. The deliberations of the expert panel took into account the fact that the key pathogenetic process in PMF is no longer idiopathic or agnogenic; PMF is now known to constitute a cl...

Journal: :iranian journal of allergy, asthma and immunology 0
soheila moradi mofid children hospital, shaheed beheshti university, tehran, iran zahra chavoshzadeh pediatric infections research center, shaheed beheshti university, tehran, iran mina izadyar department of pediatrics, pediatrics center of excellence, children's medical center, tehran univers fatemeh mahjoub division of pathology, children's medical center, tehran university of medical sciences, tehran, ira nima rezaei growth and development research center, tehran university of medical sciences, tehran, iran

idiopathic cd4+ lymphocytopenia is a rare combined immunodeficiency disease, characterized by low cd4+ t-cell count and increased susceptibility to opportunistic infections, autoimmunity and malignancies after exclusion of secondary forms of cd4 lymphocytopenia. here we present a 13-year old boy who was referred to our center because of destructive ulceration of soft and hard palates with exten...

Journal: :iranian red crescent medical journal 0
farkhondeh behjati genetics research center, university of social welfare and rehabilitation sciences, tehran, ir iran saghar ghasemi firouzabadi genetics research center, university of social welfare and rehabilitation sciences, tehran, ir iran firoozeh sajedi pediatric neurorehabilitation research center, university of social welfare and rehabilitation sciences, tehran, ir iran kimia kahrizi genetics research center, university of social welfare and rehabilitation sciences, tehran, ir iran mostafa najafi genetics research center, university of social welfare and rehabilitation sciences, tehran, ir iran behruz ebrahimizade ghasemlou genetics research center, university of social welfare and rehabilitation sciences, tehran, ir iran

materials and methods a number of 100 patients with imr, normal karyotypes and negative fragile-x and metabolic tests were screened for subtelomeric abnormalities using mlpa technique. results nine of 100 patients showed subtelomeric abnormalities with at least one of the two mlpa kits. deletion in a single region was found in 3 patients, and in two different subtelomeric regions in 1 patient. ...

2013
Melissa Matzumura Javier Arias-Stella James E. Novak

Erdheim-Chester disease (ECD) is a rare, xanthogranulomatous, non-Langerhans cell histiocytosis with frequent systemic involvement. Although the diagnosis is based on characteristic histological and radiological findings, its identification can be challenging because of its heterogeneous presentation. Osteosclerosis of long bones, often associated with bone pain, is the most common initial mani...

Journal: :Clinical and experimental rheumatology 2008
F Dybowski N Sepp H J Bergerhausen J Braun

Schnitzler's syndrome is a rather rare disease which may appear in a rheumatologist's office because patients often report rheumatic symptoms with joint, bone and muscle pain. However, it is characterized by chronic urticaria, recurrent fever, liver and spleen enlargement, osteosclerosis, and lymphadenopathy, in conjunction with a serum IgM M component. A patient who had been treated with relat...

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